No abstract available
Publication types
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Case Reports
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Video-Audio Media
MeSH terms
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Child
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Haploinsufficiency / genetics*
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Humans
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MEF2 Transcription Factors / genetics
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Male
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Mutation / genetics*
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Stereotypic Movement Disorder / genetics*
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Stereotypic Movement Disorder / physiopathology*
Substances
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MEF2 Transcription Factors
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MEF2C protein, human